Eurofins

Eurofins

Senior Quality Specialist

Lancaster, PA, United States · Senior · Full-time

Sponsorship not specifiedDetected 21 hours ago
Clinical TrialsPharmacologyGMPBioinformaticsResearchCommunicationWritingAdaptabilityOrganizational SkillsMicrosoft Office

About the role

  • Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable.
  • The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services.
  • In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries.

Responsibilities

  • It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations.
  • It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.

Requirements

  • Bachelor's degree in a science-related field or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major)
  • Minimum three years of laboratory experience with knowledge of regulatory requirements
  • The Ideal Candidate would possess:

Nice to have

  • Strong computer, scientific, quality orientation, and organizational skills
  • Excellent communication (oral and written) and attention to detail
  • Word processing, spreadsheets, PowerPoint, and database experience
  • Previous GMP, Root Cause Analysis, and technical writing experience

Skills

  • Applies GMP/GLP/ISO IEC 17025 in all areas of responsibility, as appropriate
  • Perform internal quality assurance audits
  • Perform review and approval of SOP's
  • Review QC data and non-conformance issues for assigned technical groups, evaluate for trends or patterns

Visa & Work Authorization

  • Authorization to work in the United States indefinitely without restriction or sponsorship

This listing is sourced directly from Eurofins's careers page and normalized into a canonical job model.